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Summary Literature (0)
DOID:0111126 - nephronophthisis 19

Disease Ontology Definition:A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the DCDC2 gene on chromosome 6p22.

Synonyms: NPHP19

Xenbase Genes : dcdc2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014537 - nephronophthisis 19


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): nephronophthisis (is_a)